Comparison · NCT00179777-6cda80a4
Nonhydrolysed Infant Formula vs Hydrolysed Infant Formula: Number of Participants With Type 1 Diabetes Mellitus
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
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ConductScience Library. Nonhydrolysed Infant Formula vs Hydrolysed Infant Formula: Number of Participants With Type 1 Diabetes Mellitus. Trial comparisons, record NCT00179777-6cda80a4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00179777-6cda80a4
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0761 | 0.0617 | 0.0934 | wilson | |
| Risk in group 2 | 0.0842 | 0.0691 | 0.102 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00811 | -0.0312 | 0.0149 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.904 | 0.679 | 1.2 | log | |
| Odds ratio, group 1 over group 2 | 0.896 | 0.656 | 1.22 | log | |
| Number needed to treat, for one fewer participant with the outcome on Nonhydrolysed Infant Formula than on Hydrolysed Infant Formula | 123 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Nonhydrolysed Infant Formula | Number of participants diagnosed with type 1 diabetes | 82 | 1,078 | OG000 |
| Group 2 | Hydrolysed Infant Formula | Number of participants diagnosed with type 1 diabetes | 91 | 1,081 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Number of Participants With Type 1 Diabetes Mellitus
- Description
Number of participants with Type 1 diabetes mellitus assessed by (1) blood glucose and HbA1c at 12 and 18 months of age, and annually from age 2 to 10 years, and (2) oral glucose tolerance test at 6 and 10 years of age and in the final year of the study.
- Time frame
- 12 and 18 months and annually from 2 years up to 14 years
- Population
- Analysis population consisted of participants with increased genetic risk (defined HLA genotypes) for type 1 diabetes
Source ClinicalTrials.gov
Trial
- Title
- TRIGR - Primary Prevention Study for Type 1 Diabetes in Children at Risk
- NCT number
- NCT00179777
- Phases
- NA
- Conditions
- Diabetes Mellitus, Type 1
- Interventions
- Hydrolysed infant formula, Nonhydrolysed infant formula
- Lead sponsor
- University of Helsinki
- Results first posted
- 2021-07-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00179777?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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